| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92670022-92670338 | Common:1; Rare:94 | ||||
| chr9:93452292-93452371 | Rare:12 | ||||
| chr9:93453543-93453687 | Rare:32 | ||||
| chr9:95055827-95056123 | Rare:60 | ||||
| chr9:95317659-95317799 | Common:1; Rare:47; Clinvar:2 | ||||
| chr9:95875432-95875703 | Common:1; Rare:92 | ||||
| chr9:95875965-95876058 | Common:5; Rare:47; Clinvar (pathogenic):1 | ||||
| chr9:96655286-96655458 | Rare:46 | ||||
| chr9:96778046-96778154 | Rare:35 | ||||
| chr9:97633271-97633437 | Rare:43 | ||||
| chr9:97633552-97633856 | Common:3; Rare:99 | ||||
| chr9:97922471-97922568 | Common:3; Rare:47 | ||||
| chr9:97938086-97938418 | Common:1; Rare:67 | ||||
| chr9:98255593-98255877 | Common:3; Rare:86 | ||||
| chr9:98943501-98943590 | Rare:14 |